JP2005536447A - Tnf−アルファを発現するアデノウイルスベクターを用いるヒト癌の処置 - Google Patents
Tnf−アルファを発現するアデノウイルスベクターを用いるヒト癌の処置 Download PDFInfo
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- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/191—Tumor necrosis factors [TNF], e.g. lymphotoxin [LT], i.e. TNF-beta
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10332—Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
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US10/001,017 US20030086903A1 (en) | 2001-11-02 | 2001-11-02 | Therapeutic regimen for treating cancer |
US10/151,633 US7214368B2 (en) | 2001-11-02 | 2002-05-17 | Therapeutic regimen for treating cancer comprising the administration of adenoviral vectors comprising a TNF-α transgene |
PCT/US2002/035042 WO2003039458A2 (fr) | 2001-11-02 | 2002-11-01 | Schema posologique therapeutique utilise dans le traitement du cancer |
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US (5) | US20030086903A1 (fr) |
EP (1) | EP1455840B1 (fr) |
JP (1) | JP2005536447A (fr) |
AT (1) | ATE419875T1 (fr) |
CA (1) | CA2465361A1 (fr) |
DE (1) | DE60230807D1 (fr) |
WO (1) | WO2003039458A2 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2011074564A1 (fr) * | 2009-12-15 | 2011-06-23 | タカラバイオ株式会社 | Procédé de fabrication d'un vecteur d'adénovirus |
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---|---|---|---|---|
US6579522B1 (en) * | 2000-06-27 | 2003-06-17 | Genvec, Inc. | Replication deficient adenoviral TNF vector |
US8071740B2 (en) | 2000-11-17 | 2011-12-06 | Vascular Biogenics Ltd. | Promoters exhibiting endothelial cell specificity and methods of using same for regulation of angiogenesis |
AU2003222427B8 (en) | 2000-11-17 | 2010-04-29 | Vascular Biogenics Ltd. | Promoters exhibiting endothelial cell specificity and methods of using same |
US8034791B2 (en) * | 2001-04-06 | 2011-10-11 | The University Of Chicago | Activation of Egr-1 promoter by DNA damaging chemotherapeutics |
EP1436313B1 (fr) | 2001-10-19 | 2010-09-22 | Vascular Biogenics Ltd. | Constructions de polynucleotides, compositions pharmaceutiques et procedes de regulation negative de l'angiogenese et de therapie anticancereuse |
US20030086903A1 (en) * | 2001-11-02 | 2003-05-08 | Genvec, Inc. | Therapeutic regimen for treating cancer |
US20040266713A1 (en) * | 2003-04-23 | 2004-12-30 | Shan Lu | Methods and compositions for solid tumor treatment |
US20050027196A1 (en) * | 2003-07-30 | 2005-02-03 | Fitzgerald Loretta A. | System for processing patient radiation treatment data |
ATE458500T1 (de) * | 2003-11-14 | 2010-03-15 | Genvec Inc | Pharmazeutische verbindung zur behandlung von lokal fortgeschrittenem primär inoperablen pankreaskarzinom (lapc). |
WO2005079294A2 (fr) | 2004-02-12 | 2005-09-01 | Neo Vista, Inc. | Methodes et appareil pour une curietherapie intra-oculaire |
DE602005024148D1 (de) * | 2004-08-25 | 2010-11-25 | Univ Chicago | Verwendung der kombination aus temozolomid und tnf-alpha zur behandlung von glioblastoma |
US8586090B2 (en) * | 2004-10-05 | 2013-11-19 | Albert Einstein College Of Medicine Of Yeshiva University | Melanin nanoshells for protection against radiation and electronic pulses |
WO2007059208A2 (fr) | 2005-11-15 | 2007-05-24 | Neovista Inc. | Procédés et appareils pour une curiethérapie intraoculaire |
US10166271B2 (en) * | 2006-06-21 | 2019-01-01 | The Regents Of The University Of California | Methods for promoting hair growth |
CN101960489A (zh) * | 2007-12-31 | 2011-01-26 | 真实成像有限公司 | 用于分析热图像的方法、设备和系统 |
CN101959456A (zh) * | 2007-12-31 | 2011-01-26 | 真实成像有限公司 | 用于成像数据的配准的系统和方法 |
US10299686B2 (en) * | 2008-03-28 | 2019-05-28 | Real Imaging Ltd. | Method apparatus and system for analyzing images |
US8663210B2 (en) | 2009-05-13 | 2014-03-04 | Novian Health, Inc. | Methods and apparatus for performing interstitial laser therapy and interstitial brachytherapy |
WO2011054811A1 (fr) | 2009-11-03 | 2011-05-12 | Santaris Pharma A/S | Traitement combiné par des antagonistes d'arn ciblant hsp-27 |
JP5980117B2 (ja) | 2009-11-09 | 2016-08-31 | ジェンヴェック,インコーポレーテッド | サルアデノウイルスベクターの増殖方法 |
US11111284B2 (en) | 2014-08-21 | 2021-09-07 | The General Hospital Corporation | Tumor necrosis factor superfamily and TNF-like ligand muteins and methods of preparing |
Family Cites Families (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3582183D1 (de) | 1984-03-06 | 1991-04-25 | Dainippon Pharmaceutical Co | Dns den menschlichen tumornekrosisfaktor kodierend und das menschliche tumornekronisfaktor-polypeptid. |
US5288852A (en) * | 1984-03-06 | 1994-02-22 | Dainippon Pharmaceutical Co., Ltd. | Human tumor necrosis factor polypeptides |
US4879226A (en) * | 1984-04-06 | 1989-11-07 | Asahi Kasei Kogyo Kabushiki Kaisha | Novel human physiologically active polypeptide |
US5662896A (en) | 1988-03-21 | 1997-09-02 | Chiron Viagene, Inc. | Compositions and methods for cancer immunotherapy |
US5763209A (en) * | 1988-09-26 | 1998-06-09 | Arch Development Corporation | Methods and materials relating to the functional domains of DNA binding proteins |
US5206152A (en) * | 1988-04-08 | 1993-04-27 | Arch Development Corporation | Cloning and expression of early growth regulatory protein genes |
US5698531A (en) * | 1989-03-31 | 1997-12-16 | The Regents Of The University Of Michigan | Treatment of diseases by site-specific instillation of cells or site-specific transformation of cells and kits therefor |
WO1991006658A2 (fr) * | 1989-10-24 | 1991-05-16 | Cetus Corporation | Systeme d'apport de proteines infectieuses |
CA2055168A1 (fr) * | 1990-11-21 | 1992-05-22 | Walter Fiers | Muteines de tnf |
CA2098849C (fr) * | 1990-12-20 | 2007-07-10 | Ralph R. Weichselbaum | Controle de l'expression de genes par rayonnement ionisant |
US6605712B1 (en) | 1990-12-20 | 2003-08-12 | Arch Development Corporation | Gene transcription and ionizing radiation: methods and compositions |
US5358866A (en) * | 1991-07-03 | 1994-10-25 | The United States Of America As Represented By The Department Of Health And Human Services | Cytosine deaminase negative selection system for gene transfer techniques and therapies |
FR2688514A1 (fr) | 1992-03-16 | 1993-09-17 | Centre Nat Rech Scient | Adenovirus recombinants defectifs exprimant des cytokines et medicaments antitumoraux les contenant. |
US5968735A (en) * | 1992-11-12 | 1999-10-19 | Max Delbruck-Centrum Fur Molekular Medizin Berlin | Vector for the expression of therapy-relevant genes |
US5271207A (en) * | 1992-11-18 | 1993-12-21 | Moshe Epstein | Dual-function nozzle head for vacuum-packaging tooling |
US5801029A (en) * | 1993-02-16 | 1998-09-01 | Onyx Pharmaceuticals, Inc. | Cytopathic viruses for therapy and prophylaxis of neoplasia |
FR2709309B1 (fr) | 1993-08-25 | 1995-11-10 | Centre Nat Rech Scient | Compositions cellulaires, préparation et utilisations thérapeutiques. |
US5631236A (en) * | 1993-08-26 | 1997-05-20 | Baylor College Of Medicine | Gene therapy for solid tumors, using a DNA sequence encoding HSV-Tk or VZV-Tk |
US5641755A (en) * | 1994-02-04 | 1997-06-24 | Arch Development Corp. | Regulation of x-ray mediated gene expression |
US5571797A (en) * | 1994-05-11 | 1996-11-05 | Arch Development Corporation | Method of inducing gene expression by ionizing radiation |
US5851806A (en) * | 1994-06-10 | 1998-12-22 | Genvec, Inc. | Complementary adenoviral systems and cell lines |
DE69535178T2 (de) | 1994-06-10 | 2006-12-14 | Genvec, Inc. | Adenoviren-vektor systeme und zelllinien |
US7592317B1 (en) * | 1994-08-11 | 2009-09-22 | The University Of Chicago | Constitutive gene expression in conjuction with ionizing radiation |
US5962424A (en) * | 1995-02-21 | 1999-10-05 | Arch Development Corporation | Methods and compositions for targeting selectins |
AU4994596A (en) | 1995-03-01 | 1996-09-18 | Cornell Research Foundation Inc. | Interdependent adenoviral vectors and methods of using same |
AU5634696A (en) | 1995-04-28 | 1996-11-18 | Genetic Therapy, Inc. | Treatment of tumors with cells expressing interferons, tumor necrosis factors, or other cytokines |
US5993800A (en) * | 1995-06-05 | 1999-11-30 | Bristol-Myers Squibb Company | Methods for prolonging the expression of a heterologous gene of interest using soluble CTLA4 molecules and an antiCD40 ligand |
US6281010B1 (en) * | 1995-06-05 | 2001-08-28 | The Trustees Of The University Of Pennsylvania | Adenovirus gene therapy vehicle and cell line |
US6254862B1 (en) * | 1997-03-03 | 2001-07-03 | Calydon, Inc. | Adenovirus vectors specific for cells expressing alpha-fetoprotein and methods of use thereof |
WO1997012623A1 (fr) | 1995-10-06 | 1997-04-10 | Arch Development Corporation | Procedes et compositions de stimulation virale d'elimination de cellules |
SK72298A3 (en) | 1995-11-28 | 1998-12-02 | Genvec Inc | Vectors and methods for gene transfer to cells |
AU2557097A (en) * | 1996-04-17 | 1997-11-07 | Board Of Regents, The University Of Texas System | Enhanced expression of transgenes |
DE69740033D1 (de) | 1996-07-03 | 2010-12-09 | Merial Inc | Rekombinanter hunde-adenovirus 2 (cav2), welcher exogene dna enthält |
CA2232743A1 (fr) | 1997-04-02 | 1998-10-02 | Smithkline Beecham Corporation | Tl5, homologue tnf |
US5981275A (en) | 1997-04-14 | 1999-11-09 | Genzyme Corporation | Transgene expression system for increased persistence |
US6100086A (en) | 1997-04-14 | 2000-08-08 | Genzyme Corporation | Transgene expression systems |
IL120979A0 (en) | 1997-06-02 | 1997-11-20 | Interpharm Lab Ltd | Glycosylated TNF |
US6171787B1 (en) | 1997-06-26 | 2001-01-09 | Abbott Laboratories | Member of the TNF family useful for treatment and diagnosis of disease |
JP2001518304A (ja) | 1997-10-01 | 2001-10-16 | ジー・ディー・サール・アンド・カンパニー | アンギオスタチン成分を含む融合タンパク質及び抗腫瘍療法におけるその使用 |
DE19747718A1 (de) | 1997-10-29 | 1999-05-06 | Baltzer Axel Wilhelm August Dr | Verfahren zur Therapie knochenresorbierender Erkrankungen mit der molekularbiologischen Methode der Gentherapie |
AU750803B2 (en) | 1997-10-29 | 2002-07-25 | University Of Pittsburgh | Use of vectors such as adenoviruses and/or adeno associated viruses and/or retroviruses and/or herpes simplex viruses and/or liposomes and/or plasmids as a vehicle for genetic information enabling mammal cells to produce agents for the treatment of bone pathologies |
CA2308575A1 (fr) | 1997-11-03 | 1999-05-14 | Tom Tsang | Vecteurs d'expression inductible par hyperthermie utiles pour la therapie genique et procedes d'utilisation de ceux-ci |
AU762493B2 (en) | 1998-03-11 | 2003-06-26 | Board Of Regents, The University Of Texas System | Induction of apoptic or cytotoxic gene expression by adenoviral mediated gene codelivery |
WO1999047690A2 (fr) | 1998-03-16 | 1999-09-23 | Introgen Therapeutics, Inc. | Vecteurs multigenes |
PT1071805E (pt) | 1998-04-24 | 2011-10-04 | Onyx Pharma Inc | Vectores adenovirais para tratamento de doença |
CA2335038A1 (fr) | 1998-06-15 | 1999-12-23 | Arch Development Corporation | Combinaison de facteurs radiotherapeutiques et anti-angiogeniques |
IL126757A0 (en) | 1998-09-07 | 1999-08-17 | Yissum Res Dev Co | Regulation of gene expression through manipulation of mRNA splicing and its uses |
US6440944B2 (en) | 1998-10-16 | 2002-08-27 | Genvec, Inc. | Methods of administering adenoviral vectors |
WO2000035455A1 (fr) * | 1998-12-15 | 2000-06-22 | Telik, Inc. | Urees heteroaryle-aryle utilisees comme antagonistes du recepteur igf-1 |
US6495130B1 (en) | 1998-12-30 | 2002-12-17 | Calydon, Inc. | Target cell-specific adenoviral vectors containing E3 and methods of use thereof |
EP1135514B1 (fr) | 1999-01-28 | 2009-05-13 | Onyx Pharmaceuticals, Inc. | Vecteurs navettes adenoviraux comportant des genes deletes dans la region e1b |
WO2001024684A2 (fr) | 1999-10-07 | 2001-04-12 | Aguilar Cordova Carlos Estuard | Methodes de traitement de tumeurs solides et de metastases par therapie genique |
US6579522B1 (en) | 2000-06-27 | 2003-06-17 | Genvec, Inc. | Replication deficient adenoviral TNF vector |
JP2004532213A (ja) | 2001-04-06 | 2004-10-21 | ザ ユニヴァーシティ オヴ シカゴ | Egr−1プロモーター活性の化学療法誘導 |
US20030086903A1 (en) * | 2001-11-02 | 2003-05-08 | Genvec, Inc. | Therapeutic regimen for treating cancer |
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2001
- 2001-11-02 US US10/001,017 patent/US20030086903A1/en not_active Abandoned
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2002
- 2002-05-17 US US10/151,633 patent/US7214368B2/en not_active Expired - Fee Related
- 2002-11-01 DE DE60230807T patent/DE60230807D1/de not_active Expired - Lifetime
- 2002-11-01 AT AT02776411T patent/ATE419875T1/de not_active IP Right Cessation
- 2002-11-01 EP EP02776411A patent/EP1455840B1/fr not_active Expired - Lifetime
- 2002-11-01 CA CA002465361A patent/CA2465361A1/fr not_active Abandoned
- 2002-11-01 WO PCT/US2002/035042 patent/WO2003039458A2/fr active Application Filing
- 2002-11-01 JP JP2003541750A patent/JP2005536447A/ja active Pending
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2007
- 2007-04-02 US US11/695,437 patent/US20070166284A1/en not_active Abandoned
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2010
- 2010-08-12 US US12/855,050 patent/US20100305199A1/en not_active Abandoned
-
2012
- 2012-04-05 US US13/439,915 patent/US20120203052A1/en not_active Abandoned
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011074564A1 (fr) * | 2009-12-15 | 2011-06-23 | タカラバイオ株式会社 | Procédé de fabrication d'un vecteur d'adénovirus |
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US20030086904A1 (en) | 2003-05-08 |
US7214368B2 (en) | 2007-05-08 |
EP1455840B1 (fr) | 2009-01-07 |
WO2003039458A2 (fr) | 2003-05-15 |
EP1455840A2 (fr) | 2004-09-15 |
US20030086903A1 (en) | 2003-05-08 |
US20070166284A1 (en) | 2007-07-19 |
CA2465361A1 (fr) | 2003-05-15 |
US20100305199A1 (en) | 2010-12-02 |
ATE419875T1 (de) | 2009-01-15 |
EP1455840A4 (fr) | 2004-12-15 |
WO2003039458A3 (fr) | 2003-11-20 |
DE60230807D1 (de) | 2009-02-26 |
US20120203052A1 (en) | 2012-08-09 |
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